TY - JOUR
T1 - Effect of hypoxia on ALDH1A1 expression in MCF-7 human breast cancer cells and its correlation with Oct-4 pluripotency gene expression
AU - Humonobe, A. I.
AU - Syahrani, R. A.
AU - Wanandi, S. I.
N1 - Publisher Copyright:
© 2018 Institute of Physics Publishing. All rights reserved.
PY - 2018/9/7
Y1 - 2018/9/7
N2 - High aldehyde dehydrogenase (ALDH) activity is a marker of breast cancer stem cells (BCSCs). Our previous studies have indicated that, under hypoxia, stemness markers, such as Oct-4, could be modulated according to the ALDH1A1 expression in BCSC ALDH+ cells, thereby increasing their pluripotency. This study aimed to analyze the correlation between ALDH1A1 expression and Oct-4 pluripotency gene expression in MCF-7 human breast cancer cells under hypoxia in comparison with that in BCSC ALDH+ cells. This study determined the mRNA levels of ALDH1A1, Oct-4, and HIF-1α in MCF-7 breast cancer cells under hypoxia using one-step qRT-PCR, followed by normalization using 18S rRNA. Oct-4 expression was also analyzed via its correlation with ALDH1A1 expression. ALDH1A1 was expressed at a significantly higher level in 6-h hypoxic cells than in the corresponding normoxic cells, albeit the expression level started declining with the incubation time. Oct-4 and HIF-1α mRNA were also expressed at significantly higher levels in 6- and 24-h hypoxic cells, followed by decline in a time-dependent manner. The expression level pattern of these three genes peaked at 6 h under hypoxia, followed by a progressive decline, thereby confirming that the cells went into a hypoxic state. Hypoxia may alter the stemness properties of MCF-7 cells by increasing ALDH1A1 expression along with Oct-4 pluripotency gene expression. This study can contribute to further research on the implications of ALDH1A1 and hypoxia in breast cancer therapy.
AB - High aldehyde dehydrogenase (ALDH) activity is a marker of breast cancer stem cells (BCSCs). Our previous studies have indicated that, under hypoxia, stemness markers, such as Oct-4, could be modulated according to the ALDH1A1 expression in BCSC ALDH+ cells, thereby increasing their pluripotency. This study aimed to analyze the correlation between ALDH1A1 expression and Oct-4 pluripotency gene expression in MCF-7 human breast cancer cells under hypoxia in comparison with that in BCSC ALDH+ cells. This study determined the mRNA levels of ALDH1A1, Oct-4, and HIF-1α in MCF-7 breast cancer cells under hypoxia using one-step qRT-PCR, followed by normalization using 18S rRNA. Oct-4 expression was also analyzed via its correlation with ALDH1A1 expression. ALDH1A1 was expressed at a significantly higher level in 6-h hypoxic cells than in the corresponding normoxic cells, albeit the expression level started declining with the incubation time. Oct-4 and HIF-1α mRNA were also expressed at significantly higher levels in 6- and 24-h hypoxic cells, followed by decline in a time-dependent manner. The expression level pattern of these three genes peaked at 6 h under hypoxia, followed by a progressive decline, thereby confirming that the cells went into a hypoxic state. Hypoxia may alter the stemness properties of MCF-7 cells by increasing ALDH1A1 expression along with Oct-4 pluripotency gene expression. This study can contribute to further research on the implications of ALDH1A1 and hypoxia in breast cancer therapy.
UR - http://www.scopus.com/inward/record.url?scp=85054537452&partnerID=8YFLogxK
U2 - 10.1088/1742-6596/1073/3/032062
DO - 10.1088/1742-6596/1073/3/032062
M3 - Conference article
AN - SCOPUS:85054537452
SN - 1742-6588
VL - 1073
JO - Journal of Physics: Conference Series
JF - Journal of Physics: Conference Series
IS - 3
M1 - 032062
T2 - 2nd Physics and Technologies in Medicine and Dentistry Symposium, PTMDS 2018
Y2 - 18 July 2018 through 18 July 2018
ER -